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Author Topic: I *mostly* passed my first round of testing!  (Read 10605 times)
treehugger
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« on: June 02, 2009, 09:11:18 AM »

My transplant coordinator just called me (my testing day was exactly 1 week ago) to give me my results. They are mostly positive.

The issues: I am slightly anemic and they want me to take an iron supplement for the duration of the evaluation period. I'm not worried about this though because I think it's connected to giving blood every 8 weeks (I have never been anemic in my life until my last 2 donations I was borderline; apparently regular donation can catch up to some people, but it corrects itself).

My EKG showed I have slight premature ventricular contractions (or something), so I need to have a follow-up heart sonogram (ECG). They don't think it's anything serious, so I'm not going to worry about this either.

And lastly, my total cholesterol is 217, but this doesn't preclude me from donating, and since I have been working my with doctor on this (and it's much, much lower than it initially was when I found out it was high 5 years ago), I'm not concerned about this.

They also can't find my blood draw (5 tubes) for my genetic markers, so I have to have that redrawn.

All in all, some pretty good results and nothing that dismisses me out of hand from being a donor. *sighs with relief*

On to the next step: trying to convince my doctor to give me the ECG, so I don't have to go back to UCSF just for that. I also have to say that I am very pleased to see that my transplant coordinator, Meredith, is really on top of things. She called me exactly when she said she would. That's worth a lot!  :2thumbsup;

Kara
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Wife and partner to CKD patient (diagnosed in 8/2002) who has been on PD since 9/2008.
Hopeful future live kidney donor (via paired exchange).
willowtreewren
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My two beautifull granddaughters

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« Reply #1 on: June 02, 2009, 03:45:44 PM »

All Right! :clap; :clap; :clap;

This is good news!
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Wife to Carl, who has PKD.
Mother to Meagan, who has PKD.
Partner for NxStage HD August 2008 - February 2011.
Carl transplanted with cadaveric kidney, February 3, 2011. :)
okarol
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« Reply #2 on: June 02, 2009, 04:01:16 PM »

 :2thumbsup; Great - I hope everything works out!!
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
David13
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« Reply #3 on: June 02, 2009, 05:26:49 PM »

So far so good, treehugger!   :2thumbsup;

By the way, I totally agree about the coordinator calling when she said.  Nothing ticks me off more than waiting for a scheduled phone call that never materializes. 
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kellyt
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« Reply #4 on: June 02, 2009, 06:02:00 PM »

Good Luck.  I'm rooting for you.   :cheer:

I can't wait for the news that ya'll have scheduled the date!
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1993 diagnosed with glomerulonephritis.
Oct 41, 2007 - Got fistula placed.
Feb 13, 2008 - Activated on "the list".
Nov 5, 2008 - Received living donor transplant from my sister-in-law, Etta.
Nov 5, 2011 - THREE YEARS POST TRANSPLANT!  :D
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